Discovering that your expected baby has a birth defect is an emotionally challenging experience. The information provided by doctors can be overwhelming, and it’s difficult to process everything. We understand that this is a heartbreaking time for you, and we want you to know that you are not alone.
At CHERUBS, we are a close-knit community of hundreds of families who have gone through similar experiences. We encourage you to explore our website and connect with other families who know exactly what you are going through. While we wish you had never heard of CDH, we are here to support you every step of the way through your journey.
Feel free to join our Forums to become an official member of our charity. Membership is free and provides access to valuable resources, including our Facebook groups, events, and more. Additionally, you’ll receive a care package filled with essential information and items needed during your hospital stay.
Learn all about CDH to increase your baby’s chances of survival and lead a normal life. We strive to use simple language on our website, so you won’t have to deal with complex medical jargon.
You can also find valuable advice, sources of financial assistance, and much more in the comprehensive CDH Parent Reference Guide. We are here to support you in every way we can, and together, we will navigate through this challenging time.